Zahn S - Search Results

1

Identification of recurrent chromosomal aberrations in germ cell tumors of neonates and infants using genomewide array-based comparative genomic hybridization.

Veltman I, Veltman J, Janssen I, Hulsbergen-van de Kaa C, Oosterhuis W, Schneider D, Stoop H, Gillis A, Zahn S, Looijenga L, Göbel U, van Kessel AG. Veltman I, et al. Among authors: zahn s. Genes Chromosomes Cancer. 2005 Aug;43(4):367-76. doi: 10.1002/gcc.20208. Genes Chromosomes Cancer. 2005. PMID: 15880464

2

Imbalances of chromosome arm 1p in pediatric and adult germ cell tumors are caused by true allelic loss: a combined comparative genomic hybridization and microsatellite analysis.

Zahn S, Sievers S, Alemazkour K, Orb S, Harms D, Schulz WA, Calaminus G, Göbel U, Schneider DT. Zahn S, et al. Genes Chromosomes Cancer. 2006 Nov;45(11):995-1006. doi: 10.1002/gcc.20363. Genes Chromosomes Cancer. 2006. PMID: 16897744

3

IGF2/H19 imprinting analysis of human germ cell tumors (GCTs) using the methylation-sensitive single-nucleotide primer extension method reflects the origin of GCTs in different stages of primordial germ cell development.

Sievers S, Alemazkour K, Zahn S, Perlman EJ, Gillis AJ, Looijenga LH, Göbel U, Schneider DT. Sievers S, et al. Among authors: zahn s. Genes Chromosomes Cancer. 2005 Nov;44(3):256-64. doi: 10.1002/gcc.20237. Genes Chromosomes Cancer. 2005. PMID: 16001432

4

Molecular genetic analysis of central nervous system germ cell tumors with comparative genomic hybridization.

Schneider DT, Zahn S, Sievers S, Alemazkour K, Reifenberger G, Wiestler OD, Calaminus G, Göbel U, Perlman EJ. Schneider DT, et al. Among authors: zahn s. Mod Pathol. 2006 Jun;19(6):864-73. doi: 10.1038/modpathol.3800607. Mod Pathol. 2006. PMID: 16607373 Free article.

5

Pathology and molecular biology of teratomas in childhood and adolescence.

Harms D, Zahn S, Göbel U, Schneider DT. Harms D, et al. Among authors: zahn s. Klin Padiatr. 2006 Nov-Dec;218(6):296-302. doi: 10.1055/s-2006-942271. Klin Padiatr. 2006. PMID: 17080330

6

Molecular genetic analysis of bilateral ovarian germ cell tumors.

Hennes E, Zahn S, Lopes LF, Schönberger S, Leuschner I, Göbel U, Calaminus G, Schneider DT. Hennes E, et al. Among authors: zahn s. Klin Padiatr. 2012 Oct;224(6):359-65. doi: 10.1055/s-0032-1327606. Epub 2012 Nov 9. Klin Padiatr. 2012. PMID: 23143763

7

Analysis of the adenomatous polyposis coli (APC) gene in childhood and adolescent germ cell tumors.

Okpanyi V, Schneider DT, Zahn S, Sievers S, Calaminus G, Nicholson JC, Palmer RD, Leuschner I, Borkhardt A, Schönberger S. Okpanyi V, et al. Among authors: zahn s. Pediatr Blood Cancer. 2011 Mar;56(3):384-91. doi: 10.1002/pbc.22669. Epub 2010 Nov 12. Pediatr Blood Cancer. 2011. PMID: 21225915

8

Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations.

Engels H, Bosse K, Ehrbrecht A, Zahn S, Hoischen A, Propping P, Bindl L, Reutter H. Engels H, et al. Among authors: zahn s. Am J Med Genet. 2002 Aug 1;111(2):205-9. doi: 10.1002/ajmg.10560. Am J Med Genet. 2002. PMID: 12210352 Review.

9

Constitutive activation of neuregulin/ERBB3 signaling pathway in clear cell sarcoma of soft tissue.

Schaefer KL, Brachwitz K, Braun Y, Diallo R, Wai DH, Zahn S, Schneider DT, Kuhnen C, Vollmann A, Brockhoff G, Gabbert HE, Poremba C. Schaefer KL, et al. Among authors: zahn s. Neoplasia. 2006 Jul;8(7):613-22. doi: 10.1593/neo.06238. Neoplasia. 2006. PMID: 16867224 Free PMC article.

10

Comprehensive analysis of human subtelomeres with combined binary ratio labelling fluorescence in situ hybridisation.

Engels H, Ehrbrecht A, Zahn S, Bosse K, Vrolijk H, White S, Kalscheuer V, Hoovers JM, Schwanitz G, Propping P, Tanke HJ, Wiegant J, Raap AK. Engels H, et al. Among authors: zahn s. Eur J Hum Genet. 2003 Sep;11(9):643-51. doi: 10.1038/sj.ejhg.5201028. Eur J Hum Genet. 2003. PMID: 12939649

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